Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36306917-36307121 | Rare:78 | ||||
chr1:36450424-36450583 | Common:1; Rare:45 | ||||
chr1:36464266-36464468 | Common:2; Rare:55 | ||||
chr1:37474373-37474584 | Common:1; Rare:83 | ||||
chr1:37692183-37692545 | Common:4; Rare:78 | ||||
chr1:37859550-37859780 | Common:3; Rare:75 | ||||
chr1:38859696-38859945 | Rare:95 | ||||
chr1:38873306-38873566 | Common:3; Rare:93 | ||||
chr1:39026243-39026397 | Common:1; Rare:41 | ||||
chr1:39954915-39955230 | Common:1; Rare:77 | ||||
chr1:40039967-40040255 | Common:3; Rare:60 | ||||
chr1:40040444-40040806 | Common:3; Rare:110 | ||||
chr1:40161135-40161402 | Common:1; Rare:67 | ||||
chr1:40257869-40258282 | Common:4; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40374566-40374681 | Common:12; Rare:27 |